Conference Date: May 27-29, 2022
Conference Venue: Xi'an, China
Website: https://www.maymeeting.org/conference/GECT2022/
Online Registration System: https://www.maymeeting.org/RegistrationSubmission/default.aspx?ConferenceID=1479
Email: wsconf5@163.com

Int'l Conference on Gene Editing and CRISPR Technologies (GECT 2022) will be held in Xi'an, China, during May 27-29, 2022. The aim of GECT is to provide a stage for researchers, engineers, academicians as well as industrial professionals from all over the world to present their research results and development activities in Biomedicine, Clinical Application of Gene Editing, CRISPR Systems and CRISPR Technologies, Effective Delivery for Genes in Vitro, Gene Knock In and Genomic Screening, Genome Engineering and DNA repair, Single Base Editing, etc. GECT 2022 will be a valuable and important platform for inspiring international and interdisciplinary exchange at the forefront of CGene Editing and CRISPR Technologies. 


If you wish to serve the conference as an invited speaker, please send email to us with your CV. We'll contact with you asap.

Publication and Presentation

Publication: Open Access Journal，please contact us for detailed information
Index: CNKI and Google Scholar
Note: If you want to present your research results but do NOT wish to publish a paper, you may simply submit an Abstract to our Registration System.

Contact Us

Email: wsconf5@163.com
Tel: +86 132 6470 2250 (From Monday to Friday)
QQ: 1349406763 
WeChat: 3025797047
Official Account: Academic Communications

Attendance Methods

1.Submit full paper (Regular Attendance+Paper Publication+Presentation)
You are welcome to submit full paper, all the accepted papers will be published by Open access journal.
2. Submit abstract (Regular Attendance+Abstract+Presentation)
3. Regular Attendance (No Submission Required) 

Conference Topics

  • Biomedicine
  • Cas Genes and CRISPR Subtypes
  • Clinical Application of Gene Editing
  • CRISPR Biology
  • CRISPR Systems and CRISPR Technologies
  • CRISPR-Associated Systems
  • Delivery and specificity of CRISPR-based tools
  • Different Gene Delivery Systems
  • Disease Models
  • Effective Delivery for Genes in Vitro
  • Gene Drive
  • Gene Editing Technology and Gene Editing Efficiency
  • Gene Editing-Based Safety and Ethics
  • Gene Function
  • Gene Knock In and Genomic Screening
  • Gene Therapy
  • Genetic Vaccines
  • Genetics and Genomic Medicine
  • Genome Editing and Genome Regulation
  • Genome Engineering and DNA repair
  • In Situ Gene Editing
  • In Vitro Genetic Depletion
  • In Vivo Gene Editing
  • Locus Structure
  • Molecular Epigenetics
  • Nano-Therapy
  • Off-Target Effects
  • Optimizing Repair of CRISPR-Generated DNA Breaks
  • Programmable Gene Expression
  • Regulatory, Safety Aspects of Cell and Gene Therapy
  • Repeated Sequences
  • RNA Editing Technology
  • RNA Guided Nuclease for Genome Modifications
  • RNAi and Gene Therapy
  • RNAi based Screening Technologies
  • Single Base Editing
  • Spacer Acquisition, Biogenesis, and Interference
  • Targeted Gene Replacement
  • Vectors for Gene Therapy
  • Viral Gene Therapy